A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14097832



Internal ID21285338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:54926888..54934788hg38UCSC Ensembl
Innerchr16:54960800..54968700hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg387901
hg197901
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111224
Supporting Variants
Samplessample372
Known GenesCRNDE, IRX5
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14097832
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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